Canonical Allele Identifier: PA2573061939
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1332557
ClinVar RCV Id: RCV001805603
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys890Arg
CA346731476
NM_000251.3:c.2669A>G